TPD study of NH3 adsorption/desorption on the surface of V/Ti, V/Al based catalysts for selective catalytic reduction of NOx by ammonia 1. TPD test of γ-Al2O3, TiO2 (anatase) and alumina-supported vanadia catalysts

1998 ◽  
Vol 65 (2) ◽  
pp. 363-370 ◽  
Author(s):  
N. M. Popova ◽  
L. A. Sokolova ◽  
E. A. Marchenko ◽  
L. N. Bobrova
Catalysts ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1035
Author(s):  
Baiyu Fan ◽  
Ziyin Zhang ◽  
Caixia Liu ◽  
Qingling Liu

The Fe/(SZr) and S(Fe/Zr) sulfated iron-based catalysts, prepared by impregnation methods through changing the loading order of Fe2O3 and SO42− on ZrO2, were investigated on selective catalytic reduction (SCR) of NOx by ammonia. It was studied that the existent forms of Fe2O3 and SO42− on the surface of catalysts were affected by the loading order. The Fe/(SZr) catalyst surface had isolated Fe2O3 and SO42− species and followed both the L-H mechanism and the E-R mechanism, whereas the S(Fe/Zr) catalyst contained SO42− specie and sulfate only and mainly followed the E-R pathway. These factors affected the redox ability and NH3 adsorption, which might be key to the SCR reaction.


Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1307 ◽  
Author(s):  
Yaping Zhang ◽  
Xiupeng Yue ◽  
Tianjiao Huang ◽  
Kai Shen ◽  
Bin Lu

TiO2-ZrO2 (Ti-Zr) carrier was prepared by a co-precipitation method and 1 wt. % V2O5 and 0.2 CeO2 (the Mole ratio of Ce to Ti-Zr) was impregnated to obtain the V2O5-CeO2/TiO2-ZrO2 catalyst for the selective catalytic reduction of NOx by NH3. The transient activity tests and the in situ DRIFTS (diffuse reflectance infrared Fourier transform spectroscopy) analyses were employed to explore the NH3-SCR (selective catalytic reduction) mechanism systematically, and by designing various conditions of single or mixing feeding gas and pre-treatment ways, a possible pathway of NOx reduction was proposed. It was found that NH3 exhibited a competitive advantage over NO in its adsorption on the catalyst surface, and could form an active intermediate substance of -NH2. More acid sites and intermediate reaction species (-NH2), at lower temperatures, significantly promoted the SCR activity of the V2O5-0.2CeO2/TiO2-ZrO2 catalyst. The presence of O2 could promote the conversion of NO to NO2, while NO2 was easier to reduce. The co-existence of NH3 and O2 resulted in the NH3 adsorption strength being lower, as compared to tests without O2, since O2 could occupy a part of the active site. Due to CeO2’s excellent oxygen storage-release capacity, NH3 adsorption was weakened, in comparison to the 1 wt. % V2O5-0.2CeO2/TiO2-ZrO2 catalyst. If NOx were to be pre-adsorbed in the catalyst, the formation of nitrate and nitro species would be difficult to desorb, which would greatly hinder the SCR reaction. All the findings concluded that NH3-SCR worked mainly through the Eley-Rideal (E-R) mechanism.


Materials ◽  
2019 ◽  
Vol 12 (16) ◽  
pp. 2534
Author(s):  
Yaping Zhang ◽  
Peng Wu ◽  
Ke Zhuang ◽  
Kai Shen ◽  
Sheng Wang ◽  
...  

The effect of SO2 on the selective catalytic reduction of NOx by NH3 over V2O5-0.2CeO2/TiO2-ZrO2 catalysts was studied through catalytic activity tests and various characterization methods, like Brunner−Emmet−Teller (BET) surface measurement, X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray fluorescence (XRF), hydrogen temperature-programmed desorption (H2-TPR), X-ray photoelectron spectroscopy (XPS) and in situ diffused reflectance infrared Fourier transform spectroscopy (DRIFTS). The results showed that the catalyst exhibited superior SO2 resistance when the volume fraction of SO2 was below 0.02%. As the SO2 concentration further increased, the NOx conversion exhibited some degree of decline but could restore to the original level when stopping feeding SO2. The deactivation of the catalyst caused by water in the flue gas was reversible. However, when 10% H2O was introduced together with 0.06% SO2, the NOx conversion was rapidly reduced and became unrecoverable. Characterizations indicated that the specific surface area of the deactivated catalyst was significantly reduced and the redox ability was weakened, which was highly responsible for the decrease of the catalytic activity. XPS results showed that more Ce3+ was generated in the case of reacting with SO2. In situ DRIFTS results confirmed that the adsorption capacity of SO2 was enhanced obviously in the presence of O2, while the SO2 considerably refrained the adsorption of NH3. The adsorption of NOx was strengthened by SO2 to some extent. In addition, NH3 adsorption was improved after pre-adsorbed by SO2 + O2, indicating that the Ce3+ and more oxygen vacancy were produced.


2020 ◽  
Vol 10 (16) ◽  
pp. 5525-5534 ◽  
Author(s):  
Jialiang Gu ◽  
Bingjun Zhu ◽  
Rudi Duan ◽  
Yan Chen ◽  
Shaoxin Wang ◽  
...  

MnOx–FeOx-Loaded silicalite-1 catalysts exhibit high NOx conversion at low temperatures.


RSC Advances ◽  
2020 ◽  
Vol 10 (67) ◽  
pp. 40948-40959
Author(s):  
Caixia Liu ◽  
Huijun Wang ◽  
Yalian Bi ◽  
Ziyin Zhang

The roles of Fe3+ and SO42− are different at low and high temperatures due to their interaction. It is the appropriate contents of Fe3+ and SO42− that can result in high NH3-SCR activity at varying temperatures.


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